CL2007002593A1 - COMPOUNDS DERIVED FROM 4-HETEROARIL-PIRIDINA; PHARMACEUTICAL COMPOSITION; AND USE IN THE TREATMENT OF SUCH DISEASES AS REJECTION OF TRANSPLANTED ORGANS, AUTOIMMUNE SYNDROMES AND CANCER. - Google Patents
COMPOUNDS DERIVED FROM 4-HETEROARIL-PIRIDINA; PHARMACEUTICAL COMPOSITION; AND USE IN THE TREATMENT OF SUCH DISEASES AS REJECTION OF TRANSPLANTED ORGANS, AUTOIMMUNE SYNDROMES AND CANCER.Info
- Publication number
- CL2007002593A1 CL2007002593A1 CL200702593A CL2007002593A CL2007002593A1 CL 2007002593 A1 CL2007002593 A1 CL 2007002593A1 CL 200702593 A CL200702593 A CL 200702593A CL 2007002593 A CL2007002593 A CL 2007002593A CL 2007002593 A1 CL2007002593 A1 CL 2007002593A1
- Authority
- CL
- Chile
- Prior art keywords
- piridina
- heteroaril
- rejection
- cancer
- diseases
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 title 1
- 230000001363 autoimmune Effects 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 210000000056 organ Anatomy 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 208000011580 syndromic disease Diseases 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Transplantation (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Emergency Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Otolaryngology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IB2006053147 | 2006-09-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2007002593A1 true CL2007002593A1 (en) | 2008-06-13 |
Family
ID=38983600
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL200702593A CL2007002593A1 (en) | 2006-09-07 | 2007-09-06 | COMPOUNDS DERIVED FROM 4-HETEROARIL-PIRIDINA; PHARMACEUTICAL COMPOSITION; AND USE IN THE TREATMENT OF SUCH DISEASES AS REJECTION OF TRANSPLANTED ORGANS, AUTOIMMUNE SYNDROMES AND CANCER. |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US8580824B2 (en) |
| EP (1) | EP2069336B1 (en) |
| JP (1) | JP5253401B2 (en) |
| KR (1) | KR101470659B1 (en) |
| CN (1) | CN101511827B (en) |
| AR (1) | AR062683A1 (en) |
| AU (1) | AU2007292993B2 (en) |
| BR (1) | BRPI0716171B8 (en) |
| CA (1) | CA2661105C (en) |
| CL (1) | CL2007002593A1 (en) |
| CY (1) | CY1113727T1 (en) |
| DK (1) | DK2069336T3 (en) |
| ES (1) | ES2400533T3 (en) |
| HR (1) | HRP20130181T1 (en) |
| IL (1) | IL197393A (en) |
| MA (1) | MA30718B1 (en) |
| MX (1) | MX2009002233A (en) |
| MY (1) | MY149853A (en) |
| NO (1) | NO342156B1 (en) |
| NZ (1) | NZ576060A (en) |
| PL (1) | PL2069336T3 (en) |
| PT (1) | PT2069336E (en) |
| RU (1) | RU2447071C2 (en) |
| SI (1) | SI2069336T1 (en) |
| TW (1) | TWI392671B (en) |
| WO (1) | WO2008029371A1 (en) |
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| BRPI0716633A2 (en) * | 2006-09-08 | 2013-09-24 | Actelion Pharmaceuticals Ltd | pyridin-3-yl derivatives, pharmaceutical composition and use of a compound as an immunomodulatory agent |
| KR20090051774A (en) | 2006-09-21 | 2009-05-22 | 액테리온 파마슈티칼 리미티드 | Phenyl derivatives and their use as immunomodulators |
| BRPI0720043A2 (en) * | 2006-12-15 | 2014-01-07 | Abbott Lab | OXADIAZOL COMPOUND |
| JO2701B1 (en) | 2006-12-21 | 2013-03-03 | جلاكسو جروب ليميتد | Compounds |
| CN101627034B (en) * | 2007-03-16 | 2013-05-15 | 埃科特莱茵药品有限公司 | Amino-pyridine derivatives as S1P1/EDG1 receptor agonists |
| PL2195311T3 (en) * | 2007-08-17 | 2011-08-31 | Actelion Pharmaceuticals Ltd | Pyridine derivatives as s1p1/edg1 receptor modulators |
| CA2700917A1 (en) * | 2007-11-01 | 2009-05-07 | Actelion Pharmaceuticals Ltd | Novel pyrimidine derivatives |
| US20110046170A1 (en) * | 2008-03-06 | 2011-02-24 | Martin Bolli | Novel pyrimidine-pyridine derivatives |
| ES2389042T3 (en) * | 2008-03-06 | 2012-10-22 | Actelion Pharmaceuticals Ltd. | Pyridine compounds |
| PL2252609T3 (en) * | 2008-03-07 | 2013-09-30 | Idorsia Pharmaceuticals Ltd | Pyridin-2-yl derivatives as immunomodulating agents |
| CA2715317A1 (en) * | 2008-03-07 | 2009-09-11 | Actelion Pharmaceuticals Ltd | Novel aminomethyl benzene derivatives |
| SI2278960T2 (en) | 2008-03-17 | 2020-02-28 | Actelion Pharmaceuticals Ltd. | Dosing regimen for a selective sip1 receptor agonist |
| TWI490214B (en) | 2008-05-30 | 2015-07-01 | 艾德克 上野股份有限公司 | Benzene or thiophene derivative and use thereof as vap-1 inhibitor |
| NZ590474A (en) | 2008-07-23 | 2012-10-26 | Arena Pharm Inc | SUBSTITUTED 1,2,3,4- TETRAHYDROCYCLOPENTA[b]INDOL-3-YL) ACETIC ACID DERIVATIVES USEFUL IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISORDERS |
| JP5726737B2 (en) | 2008-08-27 | 2015-06-03 | アリーナ ファーマシューティカルズ, インコーポレイテッド | Substituted tricyclic acid derivatives as agonists of S1P1 receptors useful in the treatment of autoimmune disorders and immune disorders |
| US8389509B2 (en) | 2009-01-23 | 2013-03-05 | Bristol-Myers Squibb Company | Substituted pyrazole compounds |
| EP2389377B1 (en) | 2009-01-23 | 2014-07-16 | Bristol-Myers Squibb Company | Substituted oxadiazole derivatives as s1p agonists in the treatment of autoimmune and inflammatory diseases |
| US8354398B2 (en) | 2009-01-23 | 2013-01-15 | Bristol-Myers Squibb Company | Substituted isoxazole compounds |
| AR075781A1 (en) * | 2009-03-03 | 2011-04-27 | Merck Serono Sa | DERIVATIVES OF OXADIAZOL PIRIDINA AS AGONISTS OF THE S1P1 / EDG1 RECEPTOR AND A METHOD FOR THEIR PREPARATION. |
| KR20120022757A (en) * | 2009-04-17 | 2012-03-12 | 이시하라 산교 가부시끼가이샤 | Method for producing 2-halogeno-6-substituted-4-trifluoromethylpyridine |
| DE102009002514A1 (en) * | 2009-04-21 | 2010-10-28 | Evonik Degussa Gmbh | Process for the preparation of substituted 1,4-quinone methides |
| ES2441845T3 (en) | 2009-07-16 | 2014-02-06 | Actelion Pharmaceuticals Ltd. | Pyridin-4-yl derivatives as S1P1 / EDG1 agonists |
| US8399451B2 (en) | 2009-08-07 | 2013-03-19 | Bristol-Myers Squibb Company | Heterocyclic compounds |
| EP4148045A1 (en) | 2010-01-27 | 2023-03-15 | Arena Pharmaceuticals, Inc. | Intermediate compounds for the preparation of (r)-2-(7-(4-cyclopentyl-3- (trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b] indol-3-yl)acetic acid and salts thereof |
| WO2011109471A1 (en) | 2010-03-03 | 2011-09-09 | Arena Pharmaceuticals, Inc. | Processes for the preparation of s1p1 receptor modulators and crystalline forms thereof |
| ES2548683T3 (en) | 2010-04-23 | 2015-10-20 | Bristol-Myers Squibb Company | 4- (5-Isoxazolyl or 5-pyrrazolyl-1,2,4-oxadiazol-3-yl) -mandelic acid amides as sphingosine-1-phosphate receptor agonists 1 |
| EP2595969B1 (en) | 2010-07-20 | 2015-04-22 | Bristol-Myers Squibb Company | Substituted 3-phenyl-1,2,4-oxadiazole compounds |
| ES2548258T3 (en) | 2010-09-24 | 2015-10-15 | Bristol-Myers Squibb Company | Oxadiazole compounds substituted and their use as S1P1 agonists |
| TWI546300B (en) * | 2011-01-19 | 2016-08-21 | 艾克泰聯製藥有限公司 | 2-methoxy-pyridin-4-yl derivative |
| RS60408B1 (en) | 2012-08-17 | 2020-07-31 | Actelion Pharmaceuticals Ltd | Process for the preparation of (2z,5z)-5-(3-chloro-4-((r)-2,3-dihydroxypropoxy)benzylidene)-2-(propylimino)-3-(o-tolyl)thiazolidin-4-one and intermediate used in said process |
| CN105189487B (en) | 2013-03-15 | 2017-12-26 | 爱杜西亚药品有限公司 | Pyridin-4-yl derivatives |
| EP4445956A3 (en) | 2015-01-06 | 2024-12-04 | Arena Pharmaceuticals, Inc. | Compound for use in treating conditions related to the s1p1 receptor |
| BR112017024785B1 (en) | 2015-05-20 | 2022-05-17 | Idorsia Pharmaceuticals Ltd | CRYSTALLINE FORM OF COMPOUND (S)-3-{4-[5-(2-CYCLOPENTYL-6-METOXY-PYRIDIN-4-YL)-[1,2,4]OXADIAZOLE-3-YL]-2-ETHYL- 6-METHYLPHENOXY}-PROPANE-1,2-DIOL, PHARMACEUTICAL COMPOSITION, AND USE |
| US10111841B2 (en) | 2015-06-19 | 2018-10-30 | University Of South Florida | Stabilization of alcohol intoxication-induced cardiovascular instability |
| PL3310760T3 (en) | 2015-06-22 | 2023-03-06 | Arena Pharmaceuticals, Inc. | Crystalline l-arginine salt of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclo-penta[b]indol-3-yl)acetic acid for use in s1p1 receptor-associated disorders |
| WO2017004609A1 (en) * | 2015-07-02 | 2017-01-05 | Exelixis, Inc. | Thiadiazole modulators of s1p and methods of making and using |
| WO2017004608A1 (en) * | 2015-07-02 | 2017-01-05 | Exelixis, Inc. | Oxadiazole modulators of s1p methods of making and using |
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| JP2002505868A (en) | 1998-03-09 | 2002-02-26 | スミスクライン・ビーチャム・コーポレイション | Human EDG-1c polynucleotides and polypeptides and uses thereof |
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- 2007-09-06 JP JP2009527264A patent/JP5253401B2/en not_active Expired - Fee Related
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- 2007-09-06 EP EP07826287A patent/EP2069336B1/en active Active
- 2007-09-06 KR KR1020097006862A patent/KR101470659B1/en not_active Expired - Fee Related
- 2007-09-06 CL CL200702593A patent/CL2007002593A1/en unknown
- 2007-09-06 RU RU2009112538/04A patent/RU2447071C2/en active
- 2007-09-06 AR ARP070103940A patent/AR062683A1/en active IP Right Grant
- 2007-09-06 SI SI200731169T patent/SI2069336T1/en unknown
- 2007-09-06 WO PCT/IB2007/053594 patent/WO2008029371A1/en not_active Ceased
- 2007-09-06 HR HRP20130181TT patent/HRP20130181T1/en unknown
- 2007-09-06 CN CN200780033152XA patent/CN101511827B/en not_active Expired - Fee Related
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- 2007-09-06 ES ES07826287T patent/ES2400533T3/en active Active
- 2007-09-06 PL PL07826287T patent/PL2069336T3/en unknown
- 2007-09-06 BR BRPI0716171A patent/BRPI0716171B8/en not_active IP Right Cessation
- 2007-09-06 US US12/310,801 patent/US8580824B2/en active Active
- 2007-09-06 CA CA2661105A patent/CA2661105C/en active Active
- 2007-09-06 TW TW096133280A patent/TWI392671B/en not_active IP Right Cessation
- 2007-09-06 PT PT78262870T patent/PT2069336E/en unknown
- 2007-09-06 MX MX2009002233A patent/MX2009002233A/en active IP Right Grant
- 2007-09-06 DK DK07826287.0T patent/DK2069336T3/en active
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2009
- 2009-03-04 IL IL197393A patent/IL197393A/en active IP Right Grant
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- 2013-02-27 CY CY20131100186T patent/CY1113727T1/en unknown
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